Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1946652Generated: November 2, 2026

Ammonia → Methyl 4-(2-(2-aminoacetamido)thiophene-3-carbonyl)benzoate

https://huagongshe.com/reaction/1946652

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantSodium IodideHCID 5238—
ReactantAcetone cardiceHCID 18522661—
ReactantMethyl 4-(2-aminothiophene-3-carbonyl)benzoateHCID 59783735—
SolventTetrahydrofuranHCID 8028—
ProductMethyl 4-(2-(2-aminoacetamido)thiophene-3-carbonyl)benzoateHCID 5978370528%

Reaction Conditions

Temperature-78 °C

Reaction Steps

In a 100 mL round-bottomed flask was dissolved title compound 491 (1 g, 2.96 mmol) and sodium iodide (0.533 g, 3.55 mmol) in tetrahydrofuran (20 mL) to give a yellow suspension. The mixture was heated at reflux for 2 hours. The mixture was cooled to −78° C. A Dewar-type condenser was attached and filled with dry ice/acetone. Ammonia was introduced as a gas and about 30 mL was condensed into the flask. The reaction mixture was left to warm up to room temperature over the weekend. The solvent was removed in vacuo and the residue was purified via ISCO (50-100% EtOAc/Hexanes; 40 g silica gel column) to obtain product as a tan powder. The solid was purified by suspending it in 1:1 dichloromethane/ether and filtering to afford title compound 492 (265 mg, 28%) as a tan powder which was sufficiently pure for the next step. MS (m/z): 319.3 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08399452B2
Source datasetuspto-grants-2013_03
ORD IDord-823085a3197549a9a36ef48fb574437c
Source noteuspto-grants-2013_03